DE69904442T2 - Cyclohexandiol-derivate - Google Patents
Cyclohexandiol-derivateInfo
- Publication number
- DE69904442T2 DE69904442T2 DE69904442T DE69904442T DE69904442T2 DE 69904442 T2 DE69904442 T2 DE 69904442T2 DE 69904442 T DE69904442 T DE 69904442T DE 69904442 T DE69904442 T DE 69904442T DE 69904442 T2 DE69904442 T2 DE 69904442T2
- Authority
- DE
- Germany
- Prior art keywords
- hydroxy
- diol
- dimethyl
- cyclohexane
- trifluoro
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- PDXRQENMIVHKPI-UHFFFAOYSA-N cyclohexane-1,1-diol Chemical class OC1(O)CCCCC1 PDXRQENMIVHKPI-UHFFFAOYSA-N 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims description 107
- 238000002360 preparation method Methods 0.000 claims description 21
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 19
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 13
- RLMGYIOTPQVQJR-UHFFFAOYSA-N cyclohexane-1,3-diol Chemical compound OC1CCCC(O)C1 RLMGYIOTPQVQJR-UHFFFAOYSA-N 0.000 claims description 9
- 208000035475 disorder Diseases 0.000 claims description 8
- 125000006239 protecting group Chemical group 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 7
- 230000002265 prevention Effects 0.000 claims description 7
- 239000004480 active ingredient Substances 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 208000017520 skin disease Diseases 0.000 claims description 6
- FPGGTKZVZWFYPV-UHFFFAOYSA-M tetrabutylammonium fluoride Chemical compound [F-].CCCC[N+](CCCC)(CCCC)CCCC FPGGTKZVZWFYPV-UHFFFAOYSA-M 0.000 claims description 6
- PKGBMNJPRJDFJA-KROAHAAKSA-N (1r,3r)-5-[(2e,9z)-12,12,12-trifluoro-11-hydroxy-7,7-dimethyl-11-(trifluoromethyl)dodeca-2,9-dienylidene]cyclohexane-1,3-diol Chemical compound FC(F)(F)C(O)(C(F)(F)F)\C=C/CC(C)(C)CCC\C=C\C=C1C[C@@H](O)C[C@H](O)C1 PKGBMNJPRJDFJA-KROAHAAKSA-N 0.000 claims description 5
- AZVMIDNMKFAJAG-VRKMBTERSA-N (1r,3r)-5-[(e)-11-hydroxy-7,7,11-trimethyldodec-2-en-9-ynylidene]cyclohexane-1,3-diol Chemical compound CC(O)(C)C#CCC(C)(C)CCC\C=C\C=C1C[C@@H](O)C[C@H](O)C1 AZVMIDNMKFAJAG-VRKMBTERSA-N 0.000 claims description 5
- JEPRGZHDISKAFV-VRKMBTERSA-N (1r,3r)-5-[(e)-11-hydroxy-7,7,11-trimethyldodec-2-enylidene]cyclohexane-1,3-diol Chemical compound CC(C)(O)CCCC(C)(C)CCC\C=C\C=C1C[C@@H](O)C[C@H](O)C1 JEPRGZHDISKAFV-VRKMBTERSA-N 0.000 claims description 5
- XCKDKBYJISIVLS-UJDIOAMCSA-N (1r,3s,5z)-4-methylidene-5-[(2e,9e)-12,12,12-trifluoro-11-hydroxy-7,7-dimethyl-11-(trifluoromethyl)dodeca-2,9-dienylidene]cyclohexane-1,3-diol Chemical compound FC(F)(F)C(O)(C(F)(F)F)/C=C/CC(C)(C)CCC\C=C\C=C1\C[C@@H](O)C[C@H](O)C1=C XCKDKBYJISIVLS-UJDIOAMCSA-N 0.000 claims description 5
- IBHTYSPIJQFKQT-VWCSXSMNSA-N (1r,3s,5z)-5-[(e)-11-hydroxy-7,7,11-trimethyldodec-2-enylidene]-4-methylidenecyclohexane-1,3-diol Chemical compound CC(C)(O)CCCC(C)(C)CCC\C=C\C=C1\C[C@@H](O)C[C@H](O)C1=C IBHTYSPIJQFKQT-VWCSXSMNSA-N 0.000 claims description 5
- 201000004681 Psoriasis Diseases 0.000 claims description 5
- 239000008194 pharmaceutical composition Substances 0.000 claims description 5
- NWGZNUOCKYVHQD-ZTWZVARISA-N (1r,3r)-5-[(2e,9e)-11-hydroxy-7,7,11-trimethyldodeca-2,9-dienylidene]cyclohexane-1,3-diol Chemical compound CC(O)(C)/C=C/CC(C)(C)CCC\C=C\C=C1C[C@@H](O)C[C@H](O)C1 NWGZNUOCKYVHQD-ZTWZVARISA-N 0.000 claims description 4
- PKGBMNJPRJDFJA-ILOVMYOISA-N (1r,3r)-5-[(2e,9e)-12,12,12-trifluoro-11-hydroxy-7,7-dimethyl-11-(trifluoromethyl)dodeca-2,9-dienylidene]cyclohexane-1,3-diol Chemical compound FC(F)(F)C(O)(C(F)(F)F)/C=C/CC(C)(C)CCC\C=C\C=C1C[C@@H](O)C[C@H](O)C1 PKGBMNJPRJDFJA-ILOVMYOISA-N 0.000 claims description 4
- MPBBMXDYNMLSLM-VUIHPWRZSA-N (1r,3s,5z)-4-methylidene-5-[(e)-12,12,12-trifluoro-11-hydroxy-7,7-dimethyl-11-(trifluoromethyl)dodec-2-enylidene]cyclohexane-1,3-diol Chemical compound FC(F)(F)C(O)(C(F)(F)F)CCCC(C)(C)CCC\C=C\C=C1\C[C@@H](O)C[C@H](O)C1=C MPBBMXDYNMLSLM-VUIHPWRZSA-N 0.000 claims description 4
- DRDFFFVMRIMFTH-YTSQDVJWSA-N (1s,3z)-3-[(e)-11-hydroxy-7,7,11-trimethyldodec-2-en-9-ynylidene]-4-methylidenecyclohexan-1-ol Chemical compound CC(O)(C)C#CCC(C)(C)CCC\C=C\C=C1\C[C@@H](O)CCC1=C DRDFFFVMRIMFTH-YTSQDVJWSA-N 0.000 claims description 4
- FFLVDVFJXUYBMV-YTSQDVJWSA-N (1s,3z)-3-[(e)-11-hydroxy-7,7,11-trimethyldodec-2-enylidene]-4-methylidenecyclohexan-1-ol Chemical compound CC(C)(O)CCCC(C)(C)CCC\C=C\C=C1\C[C@@H](O)CCC1=C FFLVDVFJXUYBMV-YTSQDVJWSA-N 0.000 claims description 4
- 206010004146 Basal cell carcinoma Diseases 0.000 claims description 4
- 206010020649 Hyperkeratosis Diseases 0.000 claims description 4
- 208000001126 Keratosis Diseases 0.000 claims description 4
- 230000003463 hyperproliferative effect Effects 0.000 claims description 4
- 230000003780 keratinization Effects 0.000 claims description 4
- 230000008832 photodamage Effects 0.000 claims description 4
- 230000008569 process Effects 0.000 claims description 4
- XCKDKBYJISIVLS-LFTBMKPKSA-N (1r,3s,5z)-4-methylidene-5-[(2e,9z)-12,12,12-trifluoro-11-hydroxy-7,7-dimethyl-11-(trifluoromethyl)dodeca-2,9-dienylidene]cyclohexane-1,3-diol Chemical compound FC(F)(F)C(O)(C(F)(F)F)\C=C/CC(C)(C)CCC\C=C\C=C1\C[C@@H](O)C[C@H](O)C1=C XCKDKBYJISIVLS-LFTBMKPKSA-N 0.000 claims description 3
- 239000003937 drug carrier Substances 0.000 claims description 3
- 239000011737 fluorine Substances 0.000 claims description 3
- 229910052731 fluorine Inorganic materials 0.000 claims description 3
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 3
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000012442 inert solvent Substances 0.000 claims description 2
- 125000005010 perfluoroalkyl group Chemical group 0.000 claims description 2
- XTTAZBGJFAPIOL-QZJSNOFBSA-N (1r,3r)-5-[(e)-12,12,12-trifluoro-11-hydroxy-7,7-dimethyl-11-(trifluoromethyl)dodec-2-enylidene]cyclohexane-1,3-diol Chemical compound FC(F)(F)C(O)(C(F)(F)F)CCCC(C)(C)CCC\C=C\C=C1C[C@@H](O)C[C@H](O)C1 XTTAZBGJFAPIOL-QZJSNOFBSA-N 0.000 claims 1
- 125000006527 (C1-C5) alkyl group Chemical group 0.000 claims 1
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 204
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 186
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 122
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 94
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 76
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 68
- 229910052681 coesite Inorganic materials 0.000 description 54
- 229910052906 cristobalite Inorganic materials 0.000 description 54
- 238000003818 flash chromatography Methods 0.000 description 54
- 239000000377 silicon dioxide Substances 0.000 description 54
- 235000012239 silicon dioxide Nutrition 0.000 description 54
- 229910052682 stishovite Inorganic materials 0.000 description 54
- 229910052905 tridymite Inorganic materials 0.000 description 54
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 47
- 229910052938 sodium sulfate Inorganic materials 0.000 description 47
- 235000011152 sodium sulphate Nutrition 0.000 description 47
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 47
- 239000012230 colorless oil Substances 0.000 description 46
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 44
- 238000005481 NMR spectroscopy Methods 0.000 description 41
- 239000002904 solvent Substances 0.000 description 40
- 239000000243 solution Substances 0.000 description 38
- 239000011541 reaction mixture Substances 0.000 description 27
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 25
- 235000019270 ammonium chloride Nutrition 0.000 description 25
- 239000000203 mixture Substances 0.000 description 23
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 22
- 238000003756 stirring Methods 0.000 description 19
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 18
- 239000012267 brine Substances 0.000 description 17
- 238000001704 evaporation Methods 0.000 description 17
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 17
- 239000012043 crude product Substances 0.000 description 16
- 239000000047 product Substances 0.000 description 16
- VEPTXBCIDSFGBF-UHFFFAOYSA-M tetrabutylazanium;fluoride;trihydrate Chemical compound O.O.O.[F-].CCCC[N+](CCCC)(CCCC)CCCC VEPTXBCIDSFGBF-UHFFFAOYSA-M 0.000 description 16
- 238000001035 drying Methods 0.000 description 15
- 230000008020 evaporation Effects 0.000 description 15
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 14
- 238000005406 washing Methods 0.000 description 13
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 12
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- 238000006243 chemical reaction Methods 0.000 description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 11
- 238000000605 extraction Methods 0.000 description 11
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 10
- 150000001299 aldehydes Chemical class 0.000 description 9
- 235000020964 calcitriol Nutrition 0.000 description 9
- 239000011612 calcitriol Substances 0.000 description 9
- GMRQFYUYWCNGIN-NKMMMXOESA-N calcitriol Chemical compound C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@@H](CCCC(C)(C)O)C)=C\C=C1\C[C@@H](O)C[C@H](O)C1=C GMRQFYUYWCNGIN-NKMMMXOESA-N 0.000 description 9
- 229960005084 calcitriol Drugs 0.000 description 9
- 238000001914 filtration Methods 0.000 description 9
- 239000000543 intermediate Substances 0.000 description 9
- 239000003921 oil Substances 0.000 description 9
- 235000019198 oils Nutrition 0.000 description 9
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 8
- 239000002808 molecular sieve Substances 0.000 description 8
- 238000010791 quenching Methods 0.000 description 8
- 230000000171 quenching effect Effects 0.000 description 8
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 8
- MCSXGCZMEPXKIW-UHFFFAOYSA-N 3-hydroxy-4-[(4-methyl-2-nitrophenyl)diazenyl]-N-(3-nitrophenyl)naphthalene-2-carboxamide Chemical compound Cc1ccc(N=Nc2c(O)c(cc3ccccc23)C(=O)Nc2cccc(c2)[N+]([O-])=O)c(c1)[N+]([O-])=O MCSXGCZMEPXKIW-UHFFFAOYSA-N 0.000 description 7
- 239000002480 mineral oil Substances 0.000 description 7
- 235000010446 mineral oil Nutrition 0.000 description 7
- 150000003710 vitamin D derivatives Chemical class 0.000 description 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 238000004128 high performance liquid chromatography Methods 0.000 description 6
- RCBVKBFIWMOMHF-UHFFFAOYSA-L hydroxy-(hydroxy(dioxo)chromio)oxy-dioxochromium;pyridine Chemical compound C1=CC=NC=C1.C1=CC=NC=C1.O[Cr](=O)(=O)O[Cr](O)(=O)=O RCBVKBFIWMOMHF-UHFFFAOYSA-L 0.000 description 6
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 6
- 235000017550 sodium carbonate Nutrition 0.000 description 6
- 229910000029 sodium carbonate Inorganic materials 0.000 description 6
- LOVRVVSIBIVFTN-VSGBNLITSA-N tert-butyl-[(1r,3r)-3-[tert-butyl(dimethyl)silyl]oxy-5-(2-diphenylphosphorylethylidene)cyclohexyl]oxy-dimethylsilane Chemical compound C1[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H](O[Si](C)(C)C(C)(C)C)CC1=CCP(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 LOVRVVSIBIVFTN-VSGBNLITSA-N 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- HJUGFYREWKUQJT-UHFFFAOYSA-N tetrabromomethane Chemical compound BrC(Br)(Br)Br HJUGFYREWKUQJT-UHFFFAOYSA-N 0.000 description 6
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 6
- 102000009310 vitamin D receptors Human genes 0.000 description 6
- 108050000156 vitamin D receptors Proteins 0.000 description 6
- VRTMGTJIPBGYBB-UHFFFAOYSA-N 5,5,9-trimethyldec-7-yne-1,9-diol Chemical compound OCCCCC(C)(C)CC#CC(C)(C)O VRTMGTJIPBGYBB-UHFFFAOYSA-N 0.000 description 5
- 241001465754 Metazoa Species 0.000 description 5
- 241000699670 Mus sp. Species 0.000 description 5
- 229930003316 Vitamin D Natural products 0.000 description 5
- QYSXJUFSXHHAJI-XFEUOLMDSA-N Vitamin D3 Natural products C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)CCCC(C)C)=C/C=C1\C[C@@H](O)CCC1=C QYSXJUFSXHHAJI-XFEUOLMDSA-N 0.000 description 5
- 201000010099 disease Diseases 0.000 description 5
- 230000002500 effect on skin Effects 0.000 description 5
- ZDYVRSLAEXCVBX-UHFFFAOYSA-N pyridinium p-toluenesulfonate Chemical compound C1=CC=[NH+]C=C1.CC1=CC=C(S([O-])(=O)=O)C=C1 ZDYVRSLAEXCVBX-UHFFFAOYSA-N 0.000 description 5
- 239000000741 silica gel Substances 0.000 description 5
- 229910002027 silica gel Inorganic materials 0.000 description 5
- 239000007858 starting material Substances 0.000 description 5
- MDDUHVRJJAFRAU-YZNNVMRBSA-N tert-butyl-[(1r,3s,5z)-3-[tert-butyl(dimethyl)silyl]oxy-5-(2-diphenylphosphorylethylidene)-4-methylidenecyclohexyl]oxy-dimethylsilane Chemical compound C1[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H](O[Si](C)(C)C(C)(C)C)C(=C)\C1=C/CP(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 MDDUHVRJJAFRAU-YZNNVMRBSA-N 0.000 description 5
- 230000000699 topical effect Effects 0.000 description 5
- 150000005671 trienes Chemical class 0.000 description 5
- 235000019166 vitamin D Nutrition 0.000 description 5
- 239000011710 vitamin D Substances 0.000 description 5
- 229940046008 vitamin d Drugs 0.000 description 5
- UXTPPMLMJJPWHP-UHFFFAOYSA-N 10,10,10-trifluoro-5,5-dimethyl-9-(trifluoromethyl)dec-7-yne-1,9-diol Chemical compound OCCCCC(C)(C)CC#CC(O)(C(F)(F)F)C(F)(F)F UXTPPMLMJJPWHP-UHFFFAOYSA-N 0.000 description 4
- ZVBSFSDFSOMMLI-UHFFFAOYSA-N 2-(8,8-dibromo-5,5-dimethyloct-7-enoxy)oxane Chemical compound BrC(Br)=CCC(C)(C)CCCCOC1CCCCO1 ZVBSFSDFSOMMLI-UHFFFAOYSA-N 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 4
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 4
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000010410 layer Substances 0.000 description 4
- -1 pentafluoropropyl Chemical group 0.000 description 4
- 238000004809 thin layer chromatography Methods 0.000 description 4
- 230000004580 weight loss Effects 0.000 description 4
- DSOLLVNCOFVAEY-QZJSNOFBSA-N (1r,3r)-5-[(e)-12,12,12-trifluoro-11-hydroxy-7,7-dimethyl-11-(trifluoromethyl)dodec-2-en-9-ynylidene]cyclohexane-1,3-diol Chemical compound FC(F)(F)C(O)(C(F)(F)F)C#CCC(C)(C)CCC\C=C\C=C1C[C@@H](O)C[C@H](O)C1 DSOLLVNCOFVAEY-QZJSNOFBSA-N 0.000 description 3
- NVBSXCPICFBCAY-ARPRRWEESA-N (1s,3z)-3-[(2e,9e)-11-hydroxy-7,7,11-trimethyldodeca-2,9-dienylidene]-4-methylidenecyclohexan-1-ol Chemical compound CC(C)(O)\C=C\CC(C)(C)CCC\C=C\C=C1\C[C@@H](O)CCC1=C NVBSXCPICFBCAY-ARPRRWEESA-N 0.000 description 3
- RISQPQPKFHCKPA-VMPITWQZSA-N (e)-10,10,10-trifluoro-9-hydroxy-5,5-dimethyl-9-(trifluoromethyl)dec-7-enal Chemical compound O=CCCCC(C)(C)C\C=C\C(O)(C(F)(F)F)C(F)(F)F RISQPQPKFHCKPA-VMPITWQZSA-N 0.000 description 3
- PAAWYMXERVZEDS-YVMONPNESA-N (z)-10,10,10-trifluoro-5,5-dimethyl-9-(trifluoromethyl)dec-7-ene-1,9-diol Chemical compound OCCCCC(C)(C)C\C=C/C(O)(C(F)(F)F)C(F)(F)F PAAWYMXERVZEDS-YVMONPNESA-N 0.000 description 3
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- YKFRUJSEPGHZFJ-UHFFFAOYSA-N N-trimethylsilylimidazole Chemical compound C[Si](C)(C)N1C=CN=C1 YKFRUJSEPGHZFJ-UHFFFAOYSA-N 0.000 description 3
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 3
- 230000004913 activation Effects 0.000 description 3
- SIPUZPBQZHNSDW-UHFFFAOYSA-N bis(2-methylpropyl)aluminum Chemical compound CC(C)C[Al]CC(C)C SIPUZPBQZHNSDW-UHFFFAOYSA-N 0.000 description 3
- 230000037396 body weight Effects 0.000 description 3
- 230000000125 calcaemic effect Effects 0.000 description 3
- 210000004027 cell Anatomy 0.000 description 3
- 239000003153 chemical reaction reagent Substances 0.000 description 3
- IJOOHPMOJXWVHK-UHFFFAOYSA-N chlorotrimethylsilane Chemical compound C[Si](C)(C)Cl IJOOHPMOJXWVHK-UHFFFAOYSA-N 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 239000000499 gel Substances 0.000 description 3
- VBZWSGALLODQNC-UHFFFAOYSA-N hexafluoroacetone Chemical compound FC(F)(F)C(=O)C(F)(F)F VBZWSGALLODQNC-UHFFFAOYSA-N 0.000 description 3
- 238000005984 hydrogenation reaction Methods 0.000 description 3
- 239000006210 lotion Substances 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- PSHKMPUSSFXUIA-UHFFFAOYSA-N n,n-dimethylpyridin-2-amine Chemical compound CN(C)C1=CC=CC=N1 PSHKMPUSSFXUIA-UHFFFAOYSA-N 0.000 description 3
- 239000012044 organic layer Substances 0.000 description 3
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- CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 1
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- ZLGIYFNHBLSMPS-ATJNOEHPSA-N shellac Chemical compound OCCCCCC(O)C(O)CCCCCCCC(O)=O.C1C23[C@H](C(O)=O)CCC2[C@](C)(CO)[C@@H]1C(C(O)=O)=C[C@@H]3O ZLGIYFNHBLSMPS-ATJNOEHPSA-N 0.000 description 1
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- SHONZQYRKMHEFV-UHFFFAOYSA-N tert-butyl-[3,3-dimethyl-7-(oxan-2-yloxy)heptoxy]-dimethylsilane Chemical compound CC(C)(C)[Si](C)(C)OCCC(C)(C)CCCCOC1CCCCO1 SHONZQYRKMHEFV-UHFFFAOYSA-N 0.000 description 1
- BCNZYOJHNLTNEZ-UHFFFAOYSA-N tert-butyldimethylsilyl chloride Chemical compound CC(C)(C)[Si](C)(C)Cl BCNZYOJHNLTNEZ-UHFFFAOYSA-N 0.000 description 1
- 125000001981 tert-butyldimethylsilyl group Chemical group [H]C([H])([H])[Si]([H])(C([H])([H])[H])[*]C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 125000001412 tetrahydropyranyl group Chemical group 0.000 description 1
- OSBSFAARYOCBHB-UHFFFAOYSA-N tetrapropylammonium Chemical compound CCC[N+](CCC)(CCC)CCC OSBSFAARYOCBHB-UHFFFAOYSA-N 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 239000012049 topical pharmaceutical composition Substances 0.000 description 1
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- 230000001988 toxicity Effects 0.000 description 1
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- IIHPVYJPDKJYOU-UHFFFAOYSA-N triphenylcarbethoxymethylenephosphorane Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)(=CC(=O)OCC)C1=CC=CC=C1 IIHPVYJPDKJYOU-UHFFFAOYSA-N 0.000 description 1
- FIQMHBFVRAXMOP-UHFFFAOYSA-N triphenylphosphane oxide Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)(=O)C1=CC=CC=C1 FIQMHBFVRAXMOP-UHFFFAOYSA-N 0.000 description 1
- 125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C403/00—Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone
- C07C403/06—Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone having side-chains substituted by singly-bound oxygen atoms
- C07C403/08—Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone having side-chains substituted by singly-bound oxygen atoms by hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/27—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
- C07C45/29—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation of hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/27—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
- C07C45/29—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation of hydroxy groups
- C07C45/292—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation of hydroxy groups with chromium derivatives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C47/00—Compounds having —CHO groups
- C07C47/02—Saturated compounds having —CHO groups bound to acyclic carbon atoms or to hydrogen
- C07C47/19—Saturated compounds having —CHO groups bound to acyclic carbon atoms or to hydrogen containing hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C47/00—Compounds having —CHO groups
- C07C47/20—Unsaturated compounds having —CHO groups bound to acyclic carbon atoms
- C07C47/26—Unsaturated compounds having —CHO groups bound to acyclic carbon atoms containing hydroxy groups
- C07C47/263—Unsaturated compounds having —CHO groups bound to acyclic carbon atoms containing hydroxy groups acyclic
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C47/00—Compounds having —CHO groups
- C07C47/20—Unsaturated compounds having —CHO groups bound to acyclic carbon atoms
- C07C47/26—Unsaturated compounds having —CHO groups bound to acyclic carbon atoms containing hydroxy groups
- C07C47/273—Unsaturated compounds having —CHO groups bound to acyclic carbon atoms containing hydroxy groups containing halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
- C07F7/1804—Compounds having Si-O-C linkages
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/07—Optical isomers
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/09—Geometrical isomers
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/14—The ring being saturated
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Dermatology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP98103346 | 1998-02-26 | ||
| PCT/EP1999/001118 WO1999043646A1 (en) | 1998-02-26 | 1999-02-20 | Cyclohexanediole derivatives |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE69904442D1 DE69904442D1 (en) | 2003-01-23 |
| DE69904442T2 true DE69904442T2 (de) | 2003-09-25 |
Family
ID=8231480
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE69904442T Expired - Lifetime DE69904442T2 (de) | 1998-02-26 | 1999-02-20 | Cyclohexandiol-derivate |
Country Status (21)
| Country | Link |
|---|---|
| US (1) | US6184422B1 (es) |
| EP (1) | EP1056716B1 (es) |
| JP (1) | JP3507435B2 (es) |
| KR (1) | KR20010041313A (es) |
| CN (1) | CN1133621C (es) |
| AR (1) | AR018120A1 (es) |
| AT (1) | ATE229503T1 (es) |
| AU (1) | AU751241B2 (es) |
| BR (1) | BR9908315A (es) |
| CA (1) | CA2320180C (es) |
| CO (1) | CO4980898A1 (es) |
| DE (1) | DE69904442T2 (es) |
| DK (1) | DK1056716T3 (es) |
| ES (1) | ES2188134T3 (es) |
| MA (1) | MA26609A1 (es) |
| MY (1) | MY133520A (es) |
| PE (1) | PE20000267A1 (es) |
| PT (1) | PT1056716E (es) |
| TR (1) | TR200002477T2 (es) |
| WO (1) | WO1999043646A1 (es) |
| ZA (1) | ZA991550B (es) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2000059855A1 (en) * | 1999-04-01 | 2000-10-12 | Esperion Therapeutics, Inc. | Ether compounds, compositions, and uses thereof |
| EP1094060B1 (en) * | 1999-10-18 | 2004-04-28 | Basilea Pharmaceutica AG | New process for the preparation of retiferol derivatives |
| US6310262B1 (en) * | 1999-10-18 | 2001-10-30 | Basilea Pharmaceutica Ag | Process for preparing retiferol derivatives |
| MXPA03004074A (es) * | 2000-11-22 | 2003-09-04 | Hoffmann La Roche | Derivados de retiferol y su uso en el tratamiento de enfermedades o trastornos de la piel asociadas con fotoda°o. |
| EP1466900B1 (en) * | 2001-12-26 | 2009-01-14 | Hiroaki Takayama | 2-substituted vitamin d derivatives |
| US6723755B2 (en) | 2002-06-12 | 2004-04-20 | Piotr Chomczynski | Method of treating rosacea |
| US7812057B2 (en) * | 2004-08-25 | 2010-10-12 | Molecular Research Center, Inc. | Cosmetic compositions |
| ES2533719T3 (es) * | 2005-08-30 | 2015-04-14 | Wisconsin Alumni Research Foundation | Análogos Des-C,D de 1alfa,25-dihidroxi-19-norvitamina D3 |
| GB0712653D0 (en) | 2007-06-28 | 2007-08-08 | Syngenta Ltd | Novel herbicides |
| CA2712748A1 (en) * | 2008-01-22 | 2009-07-30 | Wisconsin Alumni Reasearch Foundation | 13,13-dimethyl-des-c,d analogs of 1.alpha.,25-dihydroxy-19-nor-vitamin d3 compounds and topical composition dosage forms and methods of treating skin conditions thereof |
| MX339746B (es) | 2009-01-27 | 2016-06-08 | Berg Llc | Vitamina d3 y análogos de la misma para aliviar efectos secundarios asociados con la quimioterapia. |
| JP5978130B2 (ja) | 2009-08-14 | 2016-08-24 | バーグ エルエルシー | 脱毛症を治療するためのビタミンｄ３およびその類似体 |
| WO2014194133A1 (en) | 2013-05-29 | 2014-12-04 | Berg Llc | Preventing or mitigating chemotherapy induced alopecia using vitamin d |
| CN114044788A (zh) * | 2021-08-12 | 2022-02-15 | 甘肃皓天医药科技有限责任公司 | 一种氟骨化醇cd环的制备方法及其应用 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2166898C (en) | 1993-07-09 | 2004-09-07 | Roger Bouillon | Novel structural analogues of vitamin d |
| PL174912B1 (pl) | 1994-01-24 | 1998-10-30 | Inst Farmaceutyczny | Nowe związki farmakologicznie czynne z grupy witamin D i sposób ich otrzymywania |
| US5461116A (en) | 1994-11-10 | 1995-10-24 | Shell Oil Company | Core functionalized star block copolymers |
| EP0983221B1 (en) * | 1997-05-23 | 2002-04-03 | Basilea Pharmaceutica AG | Cyclohexanediol derivatives |
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1999
- 1999-02-18 US US09/252,508 patent/US6184422B1/en not_active Expired - Lifetime
- 1999-02-20 AU AU26246/99A patent/AU751241B2/en not_active Ceased
- 1999-02-20 EP EP99906250A patent/EP1056716B1/en not_active Expired - Lifetime
- 1999-02-20 PT PT99906250T patent/PT1056716E/pt unknown
- 1999-02-20 JP JP2000533405A patent/JP3507435B2/ja not_active Expired - Fee Related
- 1999-02-20 AT AT99906250T patent/ATE229503T1/de not_active IP Right Cessation
- 1999-02-20 DK DK99906250T patent/DK1056716T3/da active
- 1999-02-20 CN CNB998033146A patent/CN1133621C/zh not_active Expired - Lifetime
- 1999-02-20 BR BR9908315-9A patent/BR9908315A/pt not_active IP Right Cessation
- 1999-02-20 TR TR2000/02477T patent/TR200002477T2/xx unknown
- 1999-02-20 ES ES99906250T patent/ES2188134T3/es not_active Expired - Lifetime
- 1999-02-20 KR KR1020007009419A patent/KR20010041313A/ko active IP Right Grant
- 1999-02-20 DE DE69904442T patent/DE69904442T2/de not_active Expired - Lifetime
- 1999-02-20 CA CA002320180A patent/CA2320180C/en not_active Expired - Fee Related
- 1999-02-20 WO PCT/EP1999/001118 patent/WO1999043646A1/en active IP Right Grant
- 1999-02-22 MA MA25470A patent/MA26609A1/fr unknown
- 1999-02-22 PE PE1999000151A patent/PE20000267A1/es not_active Application Discontinuation
- 1999-02-24 MY MYPI99000648A patent/MY133520A/en unknown
- 1999-02-24 CO CO99011496A patent/CO4980898A1/es unknown
- 1999-02-24 AR ARP990100773A patent/AR018120A1/es not_active Application Discontinuation
- 1999-02-25 ZA ZA9901550A patent/ZA991550B/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| KR20010041313A (ko) | 2001-05-15 |
| MY133520A (en) | 2007-11-30 |
| PE20000267A1 (es) | 2000-04-10 |
| TR200002477T2 (tr) | 2001-03-21 |
| JP2002504537A (ja) | 2002-02-12 |
| CA2320180A1 (en) | 1999-09-02 |
| CN1291974A (zh) | 2001-04-18 |
| EP1056716B1 (en) | 2002-12-11 |
| BR9908315A (pt) | 2000-11-07 |
| AU751241B2 (en) | 2002-08-08 |
| MA26609A1 (fr) | 2004-12-20 |
| DK1056716T3 (da) | 2003-04-07 |
| CA2320180C (en) | 2005-06-07 |
| WO1999043646A1 (en) | 1999-09-02 |
| CN1133621C (zh) | 2004-01-07 |
| DE69904442D1 (en) | 2003-01-23 |
| EP1056716A1 (en) | 2000-12-06 |
| JP3507435B2 (ja) | 2004-03-15 |
| PT1056716E (pt) | 2003-04-30 |
| AU2624699A (en) | 1999-09-15 |
| CO4980898A1 (es) | 2000-11-27 |
| AR018120A1 (es) | 2001-10-31 |
| ATE229503T1 (de) | 2002-12-15 |
| US6184422B1 (en) | 2001-02-06 |
| ES2188134T3 (es) | 2003-06-16 |
| ZA991550B (en) | 1999-08-26 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8364 | No opposition during term of opposition |